Ophthalmic Genetics,volume 21,issue 2  (06-2014)

Period of time: 2014年2期

Publisher: Informa Healthcare

Founded in: 1981

Total resources: 61

ISSN: 1381-6810

Subject: R77 Ophthalmology

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Ophthalmic Genetics,volume 21,issue 2

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Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene

By Eksandh Louise,Ponjavic Vesna,Munroe Patricia B.,Eiberg Hans,Uvebrant Paul,Ehinger Berndt,Mole Sara E.,Andréasson Sten in (2000)

Ophthalmic Genetics,volume 21,issue 2 , Vol. 21, Iss. 2, 2000-06 , pp. 69-77

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Homozygous and heterozygous Gly-188-Arg mutation of the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa

By Reig Carlos,Trujillo M. José,Martinez-Gimeno Maria,Garcia-Sandoval Blanca,Calvo M. Teresa,Ayuso Carmen,Carballo Miguel in (2000)

Ophthalmic Genetics,volume 21,issue 2 , Vol. 21, Iss. 2, 2000-06 , pp. 79-87

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An unusual central retinal dystrophy associated with ichthyosis vulgaris

By Saatci A. Osman,Özbek Zeynep,Köse Süheyla,Durak Ismet,Kavukçu Salih in (2000)

Ophthalmic Genetics,volume 21,issue 2 , Vol. 21, Iss. 2, 2000-06 , pp. 101-107

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Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2)

By Beneyto Magdalena,Cuevas José M.,Millán José M.,Espinós Carmen,Mateu Emilia,González-Cabo Pilar,Baiget Montserrat,Doménech Montserrat,Bernal Sara,Ayuso Carmen,García-Sandoval Blanca,Trujillo Ma José,Borrego Salud,Antiñolo Guillermo,Carballo Miguel,Nájera Carmen in (2000)

Ophthalmic Genetics,volume 21,issue 2 , Vol. 21, Iss. 2, 2000-06 , pp. 123-128

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